|
Status |
Public on Jan 01, 2009 |
Title |
3h post DNA Damage P53 Wt MEFs |
Sample type |
RNA |
|
|
Source name |
P53 Inducible MEFs
|
Organism |
Mus musculus |
Characteristics |
CRE-LOX inducible P53 WT cells were exposed to a DNA damaging agent (Doxyrubicin) and profiled across time.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was isolated using TRIzol (Invitrogen). The RNA was treated with DNaseI (Roche) before 2ug of each was used to generate cDNA with the Superscript III kit (Invitrogen). Poly-T was used to prime the cDNA synthesis. The cDNA was purified with phenol chloroform isoamyl alcohol and precipitated before being sent to Nimblegen to be analyzed for gene expression.
|
Label |
Biotin
|
Label protocol |
Nimblegen ChIP labeling protocol (http://www.nimblegen.com)
|
|
|
Hybridization protocol |
Nimblegen Hybridization protocol (http://www.nimblegen.com)
|
Scan protocol |
Arrays were scanned using AXON 5uM scanner
|
Description |
Total RNA poly-A labeled RNA were hybridized to custom arrays
|
Data processing |
Probe signal intensity (ie, Sample VALUEs) obtained using the NimbleScan software provided by Nimblegen. The .gff files (linked below as supplementary files) were also generated with NimbleScan.
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|
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Submission date |
Nov 29, 2008 |
Last update date |
Dec 09, 2008 |
Contact name |
Mitchell Guttman |
E-mail(s) |
mguttman@mit.edu
|
Organization name |
Broad Institute
|
Street address |
7 Cambridge Center
|
City |
Cambridge |
State/province |
MA |
ZIP/Postal code |
02139 |
Country |
USA |
|
|
Platform ID |
GPL7708 |
Series (1) |
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